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Creutzfeldt-Jakob

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Search Period All yearsLast 12 monthsLast 5 years Topic All topicsGeneralNutrition and dietAlternative treatment methods Type of research Any type of researchHighest quality evidence only (18)Meta-analysis (4)Systematic review (13)Phase 3 study (1)Clinical trial (24)Review article (145)Early study (phase 1 or 2) (3)Case report (262)Laboratory or animal research (18)Commentary or editorial (48) Studies currently seeking participants only (7)

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Publications and studies (1022)

• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. The role of synaptic biomarkers in the spectrum of neurodegenerative diseases. (2020/07/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An Atypical Presentation of Creutzfeldt-Jakob Disease With a Heidenhain Variant and Balint's Syndrome. (2020/06/13) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Cerebrospinal fluid neurofilament light chain is elevated in Niemann-Pick type C compared to psychiatric disorders and healthy controls and may be a marker of treatment response. (2020/06/01) ♡
• Network mediation of pathology pattern in sporadic Creutzfeldt-Jakob disease. (2020/05/15) ♡
• Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases. (2020/04/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Elucidating Critical Proteinopathic Mechanisms and Potential Drug Targets in Neurodegeneration. (2020/04/01) ♡
• Selective neuronal vulnerability is involved in cerebellar lesions of Guinea pigs infected with bovine spongiform encephalopathy (BSE) prions: Immunohistochemical and electron microscopic investigations. (2020/04/01) ♡
• Validation of Poly(Propylene Imine) Glycodendrimers Towards Their Anti-prion Conversion Efficiency. (2020/04/01) ♡
• [The fantastic story of the incredible prion]. (2020/04/01) ♡
• Prion protein codon 129 polymorphism in mild cognitive impairment and dementia: the Rotterdam Study. (2020/03/20) ♡
• Markers of A1 astrocytes stratify to molecular sub-types in sporadic Creutzfeldt-Jakob disease brain. (2020/03/17) ♡
• Person and ethics of a psychiatrist during National Socialism: Friedrich Meggendorfer (1880-1953). (2020/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Hallucinatory palinopsia and paroxysmal oscillopsia as initial manifestations of sporadic Creutzfeldt-Jakob disease: A case study. (2020/03/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Metal homeostasis disturbances in neurodegenerative disorders, with special emphasis on Creutzfeldt-Jakob disease - Potential pathogenetic mechanism and therapeutic implications. (2020/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Genetic Creutzfeldt-Jakob disease mimicking dementia with Lewy bodies: Clinical and radiological findings. (2020/02/15) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A case of M232R genetic Creutzfeldt-Jakob disease with Lewy bodies. (2020/02/15) ♡
• Neutralizing Mutations Significantly Inhibit Amyloid Formation by Human Prion Protein and Decrease Its Cytotoxicity. (2020/02/14) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Neuropathology of Lewy body disease: Clinicopathological crosstalk between typical and atypical cases. (2020/02/01) ♡
• Cerebrospinal fluid non-phosphorylated tau in the differential diagnosis of Creutzfeldt-Jakob disease: a comparative prospective study with 14-3-3. (2020/02/01) ♡
• Self-assembly hollow manganese Prussian white nanocapsules attenuate Tau-related neuropathology and cognitive decline. (2020/02/01) ♡
• Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease. (2020/01/15) ♡
• A pilot study of the utility of cerebrospinal fluid neurofilament light chain in differentiating neurodegenerative from psychiatric disorders: A 'C-reactive protein' for psychiatrists and neurologists? (2020/01/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Prion disease and recommended procedures for flexible endoscope reprocessing - a review of policies worldwide and proposal for a simplified approach. (2020/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Prion Problem: A Rapidly Progressive Dementia. (2020/01/01) ♡
• Inactivation Methods for Prions. (2020/01/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Introduction to Current Progress in Advanced Research on Prions. (2020/01/01) ♡
• Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy. (2020/01/01) ♡
• Metabolic Changes Detected by 18F-FDG PET in the Preclinical Stage of Familial Creutzfeldt-Jakob Disease. (2020/01/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Strain variation in treatment and prevention of human prion diseases. (2020/01/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. The utility of bank voles for studying prion disease. (2020/01/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. A Review of Neuroimaging in Rare Neurodegenerative Diseases. (2020/01/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia. (2019/12/31) ♡
• Identification of circulating microRNA signatures as potential biomarkers in the serum of elk infected with chronic wasting disease. (2019/12/23) ♡
• Postmortem Quantitative Analysis of Prion Seeding Activity in the Digestive System. (2019/12/16) ♡
• Quaking-induced conversion of prion protein on a thermal mixer accelerates detection in brains infected with transmissible spongiform encephalopathy agents. (2019/12/12) ♡
• Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Movement Disorders in Prionopathies: A Systematic Review. (2019/12/12) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. The first reported case of Creutzfeldt-Jakob disease from Nepal. (2019/12/12) ♡
• Two distinct prions in fatal familial insomnia and its sporadic form. (2019/12/09) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Genetic Factors in Mammalian Prion Diseases. (2019/12/03) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob Disease Mimicking Neurosyphilis: A Complex Presentation, Histopathological Findings, and Special Precautions for Autopsy. (2019/12/01) ♡
• Impact of pyridine-2-carboxaldehyde-derived aroylhydrazones on the copper-catalyzed oxidation of the M112A PrP(103-112) mutant fragment. (2019/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease with spongiform changes of the cerebral cortex. (2019/12/01) ♡
• Diagnostic value of surrogate CSF biomarkers for Creutzfeldt-Jakob disease in the era of RT-QuIC. (2019/12/01) ♡
• Domain-specific Quantification of Prion Protein in Cerebrospinal Fluid by Targeted Mass Spectrometry. (2019/12/01) ♡
• A Case of Creutzfeldt-Jakob Disease Presented as Rapid Progressive Parkinsonism. (2019/12/01) ♡
• Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients. (2019/11/28) ♡
• Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons. (2019/11/12) ♡
• Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification. (2019/11/01) ♡
• The association of quantitative EEG and MRI in Creutzfeldt-Jakob Disease. (2019/11/01) ♡
• Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome. (2019/11/01) ♡

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